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Robert Goodman a Department of Child and Adolescent Psychiatry,
Institute of Psychiatry, King's College London, London SE5 8AF, b Office for National
Statistics, London SW1V 2QQ Correspondence to: Robert Goodman r.goodman{at}iop.kcl.ac.uk
In a recent national survey, the prevalence of psychiatric
disorder in children and adolescents in Great Britain was more than
9%.1 Parents and doctors commonly think that these
disorders are transient, but longitudinal studies show
otherwise.2 We followed up children from the national
survey to examine persistence in a large sample of children in
Britain.1
The original survey studied a sample of 10 438 British children
aged 5-15 years.1 We sent the parents of all children with a psychiatric disorder (936) and a third of those without a psychiatric disorder (3029) a questionnaire. It included the strengths and difficulties questionnaire, a well validated measure of childhood psychopathology and its impact on the child.
3 4
A total of 73% of parents responded; most losses were
non-contacts, not refusals. The response rate was lower among those with a child with a disorder than those without (66% v
76%). Non-responders at follow up had had significantly more symptoms
initially (analysis of variance adjusting for initial diagnosis,
F=39.9, 1 df, P<0.001: the mean symptom score for non-responders was
greater, by 1.2, than for responders, matched by diagnosis).
Responders' and non-responders' initial impact scores did not differ
significantly. Overall, differential non-response will not have
led us to overestimate the persistence of psychopathology.
The figure shows symptom and impact scores in children initially
diagnosed with hyperkinetic, conduct, emotional, or no disorder. We
used paired t tests to test whether the changes in symptom and impact scores in children with hyperkinetic, conduct, emotional, or
no disorder were significant. For conduct disorder, neither symptoms
nor impact changed significantly. Symptoms (P<0.05) but not impact
fell significantly in children with hyperkinesis. For emotional
disorder, there were significant falls in both symptoms and impact
(P<0.001 for both), though the follow up scores were still
substantially greater than in the group with no initial disorder
(P<0.001, independent samples t
test).
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Participants, method, and results
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Participants, method, and...
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References

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Mean symptom and impact scores initially and at 18 month follow up from
the strengths and difficulties questionnaire, completed by parents, for
children with and without initial psychiatric disorder
We defined "caseness" from the combination of raised symptom
(
14) and impact scores (
2).3 Caseness at follow up
was considered informative for only the 86% (2487/2901) of
participants in whom caseness was congruent with the initial
psychiatric diagnosis. For example, when a child was initially
diagnosed as having conduct disorder solely on the basis of symptoms
reported by a teacher, and when the initial questionnaire, completed by
the parents, described their child as normal, then the diagnosis
(disorder present) and the caseness (negative) were not congruent. So,
caseness was not considered informative at follow up, since the
parent's answers to the questionnaire would probably not change
whether or not the conduct disorder persisted or was resolved.
Similarly, if the initial diagnosis of depression in a teenager was
based on self reported symptoms (not reported by a parent), the follow up parent questionnaire is unlikely to be informative.
Caseness criteria at the 18 month follow up were met by 3% (67/2249)
of children who did not initially have a psychiatric disorder, compared
with 62% (147/238) of children who did (relative risk 20.7; 95%
confidence interval 16.0 to 26.7). Persistence at 18 months varied with
initial diagnosis: 36% (25/70) for children who had an emotional
disorder initially, compared with 73% (122/168) for children with
other disorders initially (mostly conduct and hyperkinetic disorders,
sometimes with coexistent emotional disorders) (P<0.001,
2 test).
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Comment |
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Childhood psychopathology is often persistent, particularly among children with conduct disorder and hyperkinesis. Although emotional disorders have a better prognosis than conduct or hyperkinetic disorders, they are not always benign: their resolution over 18 months is far from complete, and recent work suggests an increased risk of similar disorders recurring in adulthood.2
Everyone in contact with children should take the symptoms of emotional
distress, behavioural difficulty, and hyperactivity seriously, as they
may impair the child's function and development and are unlikely to be
transient. This is particularly important as evidence based
interventions can alleviate distress and minimise the secondary
handicap that results from disrupted education and impaired social
development.5
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Acknowledgments |
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Contributors: HM directed the initial survey and the follow up and discussed the analyses, findings, and draft versions of the paper. RG and TF were on the steering committee for both surveys. RG performed the analyses while TF took the lead in drafting the paper. RG is guarantor.
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Footnotes |
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Funding. TF is funded by a Wellcome clinical training fellowship and the original surveys were funded by the Department of Health.
Competing interests: None declared.
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References |
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| 1. | Meltzer H, Gatward R, Goodman R, Ford T. Mental health of children and adolescents in Great Britain. Stationery Office: London, 2000. |
| 2. |
Harrington R.
Developmental continuities and discontinuities.
Br J Psychiatry
2001;
179:
189-190 |
| 3. | Goodman R. The extended version of the strengths and difficulties questionnaire as a guide to child psychiatric caseness and consequent burden. J Child Psychol Psychiatry 1999; 40: 791-801[CrossRef][Web of Science][Medline]. |
| 4. | Goodman R. Psychometric properties of the strengths and difficulties questionnaire (SDQ). J Am Acad Child Adolesc Psychiatry 2001; 40: 1337-1345[CrossRef][Web of Science][Medline]. |
| 5. |
Graham P.
Treatment interventions and findings from research: bridging the chasm in child psychiatry.
Br J Psychiatry
2000;
176:
414-419 |
(Accepted 27 February 2002)